A techno-economical assessment of treatment by coagulation-flocculation with aluminum and iron-bases coagulants of landfill leachate membrane concentrates.

Landfill leachate treatment involved with the membrane bioreactor (MBR) combined with membrane treatment via nanofiltration (NF) and/or reverse osmosis (RO) is widely used in Turkey. This treatment produces landfill leachate membrane concentrates (LLMCs) with an undesirably high concentration of contaminants. In the study, two different nanofiltration concentrates of leachate were coagulated. Coagulant dosages from 0.10 to 5.0 g of Me3+/L (Me3+: Al3+ or Fe3+), and the pH values ranged from 4.0 to 8.0 and 3.0-9.0 for Al-based and Fe-based coagulants, respectively. The most efficient pH values were 5.0 and 4.0 for Al3+ and Fe3+, respectively. These pH values are lower than those known to be effective in coagulants. The reason for this is the presence of humic substances in the wastewater. The cost of Fe2(SO4)3.xH2O was the lowest than other coagulants at the end of the cost analyses obtained from Istanbul region landfill leachate NF concentrate (NFCL-1) and Kocaeli region landfill leachate NF concentrate (NFCL-2). Under optimum conditions, the costs for NFCL-1 and NFCL-2 were calculated as 0.55 and 0.46 $/removed kg COD, respectively.

MOF-Based Mycotoxin Nanosensors for Food Quality and Safety Assessment through Electrochemical and Optical Methods.

Mycotoxins in food are hazardous for animal and human health, resulting in food waste and exacerbating the critical global food security situation. In addition, they affect commerce, particularly the incomes of rural farmers. The grave consequences of these contaminants require a comprehensive strategy for their elimination to preserve consumer safety and regulatory compliance. Therefore, developing a policy framework and control strategy for these contaminants is essential to improve food safety. In this context, sensing approaches based on metal-organic frameworks (MOF) offer a unique tool for the quick and effective detection of pathogenic microorganisms, heavy metals, prohibited food additives, persistent organic pollutants (POPs), toxins, veterinary medications, and pesticide residues. This review focuses on the rapid screening of MOF-based sensors to examine food safety by describing the main features and characteristics of MOF-based nanocomposites. In addition, the main prospects of MOF-based sensors are highlighted in this paper. MOF-based sensing approaches can be advantageous for assessing food safety owing to their mobility, affordability, dependability, sensitivity, and stability. We believe this report will assist readers in comprehending the impacts of food jeopardy exposure, the implications on health, and the usage of metal-organic frameworks for detecting and sensing nourishment risks.

The protective effect of natural phenolic compound on the functional and structural responses of inhibited catalase by a common azo food dye.

In this research retrieval effects of natural yellow (NY) on the performance of carmoisine (CAR) inhibited bovine liver catalase (BLC) was studied using multispectral and theoretical methods. Kinetic studies showed that CAR inhibited BLC through competitive inhibition (IC50 value of 2.24 × 10-6 M) while the addition of NY recover the activity of CAR-BLC up to 82% in comparison with the control enzyme. Circular dichroism data revealed that NY can repair the structural changes of BLC, affected by CAR. Furthermore, an equilibrium dialysis study indicated that NY could reduce the stability of the CAR-catalase complex. The surface plasmon resonance (SPR) data analysis indicated a high affinity of NY to BLC compared to CAR and the binding of NY led to a decrease in the affinity of the enzyme to the inhibitor. On the other hand, fluorescence and molecular docking studies showed that the quenching mechanism of BLC by CAR occurs through a static quenching process, and van der Waals forces and hydrogen bonding play a crucial role in the binding of CAR to BLC. MLSD data demonstrated that NY could increase the binding energy of CAR-BLC complex from -7.72 kJ mol-1 to -5.9 kJ mol-1, leading to complex instability and catalase activity salvage.

A review of boron removal from aqueous solution using carbon-based materials: An assessment of health risks.

Carbon-based compounds have gained attention of researchers for use in boron removal due to their properties, which make them a viable and low cost adsorbent with a high availability, as well as environmental friendliness and high removal efficiency. The removal of boron utilizing carbon-based materials, including activated carbon (AC), graphene oxide (GO), and carbon nanotubes (CNTs), is extensively reviewed in this paper. The effects of the operating conditions, kinetics, isotherm models, and removal methods are also elaborated. The impact of the modification of the lifetime of carbon-based materials has also been explored. Compared to unmodified carbon-based materials, modified materials have a significantly higher boron adsorption capability. It has been observed that adding various elements to carbon-based materials improves their surface area, functional groups, and pore volume. Tartaric acid, one of these doped elements, has been employed to successfully improve the boron removal and adsorption capabilities of materials. An assessment of the health risk posed to humans by boron in treated water utilizing carbon-based materials was performed to better understand the performance of materials in real-world applications. Furthermore, the boron removal effectiveness of carbon-based materials was evaluated, as well as any shortcomings, future perspectives, and gaps in the literature.

A green and sensitive guanine-based DNA biosensor for idarubicin anticancer monitoring in biological samples: A simple and fast strategy for control of health quality in chemotherapy procedure confirmed by docking investigation.

Drug efficiency can be considerably boosted while adverse effects can be reduced by precisely monitoring the concentration of anti-cancer drugs. Thus, one of the most important parameters for human health is the monitoring and detection of anticancer drugs during chemotherapy treatment. Herein, a glassy carbon electrode (GCE) was modified by Pt- and Pd-incorporated ZnO nanoparticles-decorated single-wall carbon nanotubes (Pt-Pd-ZnO/SWCNTs) nanocomposites, and ds-DNA (Calf Thymus) that was a biological recognition element, and it was aimed to be utilized as an ultrasensitive and effective electroanalytical biosensor for idarubicin (IDR) monitoring. Various physicochemical characterization techniques including transmission electron microscopy (TEM), field-emission scanning electron microscopy (FE-SEM) with energy-dispersive X-ray spectroscopy (EDS) were used to investigate the morphology and structure of the Pt-Pd-ZnO/SWCNTs nanocomposite, which was produced via straightforward chemical precipitation combined with the one-pot method. The layer-by-layer modification technique was implemented to fabricate the ds-DNA/Pt-Pd-ZnO/SWCNTs/GCE to be further utilized as a voltammetric sensor for sensitive monitoring of idarubicin in biological fluids and pharmaceutical substances. The electroanalytical method implemented to detect idarubicin was based to detect the ds-DNA's guanine base signal on the surface of the modified electrode in the absence and presence of the anticancer drug. The results explicated that the developed biosensor performed well in determining idarubicin in concentrations ranging from 1.0 nM to 65 µM, with a detection limit of 0.8 nM. The idarubicin detection ability of the modified electrode in real samples was evaluated, and the recovery data was acquired in the range of 98.0% and 104.75%. In the final step, the preferential intercalative binding mode of idarubicin drug with ds-DNA was approved by molecular docking study. This study paves the way for engineering highly sensitive DNA biosensors to be employed in the monitoring of anticancer drugs by combining the benefits of nanocomposites and valuable information of a molecular docking study.

A global systematic review on the concentration of organophosphate esters in water resources: Meta-analysis, and probabilistic risk assessment.

Organophosphate esters (OPEs) are used as additives in various industries. They do not chemically bond with the polymeric structure of materials, so they can stay for a long time and have a very adverse effect on the environment. To analyze the development of the prevalence and concentration of OPEs such as TCEP, TCPP, TDCP, TnBP, TPHP, TBOEP, TEHP, TMP, TCIPP, TDCIPP, TMPP, and TDBPP in water resources, a search between January 01, 2000, to April 08, 2021, was followed by a systematic review and meta-analysis. Among of the 888 articles scanned in the identity step, 58 articles containing 2676 samples, 10 countries, and 4 water types were included in the meta-analysis study. Among all studied OPEs, the concentration of TcrP, TCPP, TDCPP, and TnBP were at the top in water resources, with values >715 µg L-1 and lowest average concentrations were obtained for TDBPP and TpeP with values <0.0004 µg L-1. The most polluted area in terms of the concentration of OPEs in water resources was China. Besides, data analysis showed that there only was carcinogenic risk for China. A Monte-Carlo simulation indicated that although these obtained averages are in the same order of magnitude as the acceptable limit, for both adults and children, 95% of the population is at risk.

The concentration of persistent organic pollutants in water resources: A global systematic review, meta-analysis and probabilistic risk assessment.

The persistent organic pollutants (POPs) are environmentally stable and highly toxic chemicals that accumulate in living adipose tissue and have a very destructive effect on aquatic ecosystems. To analyze the evolution of the concentration and prevalence of POPs such as α-HCH, ß-HCH, γ-HCH, ∑-HCH, Heptachlor, Aldrin, p,p'-DDE, p,p'-DDT, ∑-DDT, and ∑-OCP in water resources, a search between January 01, 1970, to February 10, 2020, was followed using a systematic review and meta-analysis prevalence. Among the 2306 explored articles in the reconnaissance step, 311 articles with 5315 exemplars, 56 countries, and 4 types of water were included in the meta-analysis study. Among all studied POPs, the concentration of p,p'-DDT in water resources was the highest, especially in drinking water resources. The overall rank order based on the concentration and prevalence of POPs were surface water > drinking water > seawater > groundwater. To identify POPs-contaminated areas, the distance from the mean relative to their distribution was considered. The most to the least polluted areas included: South Africa, India, Turkey, Pakistan, Canada, Hong Kong, and China. The highest carcinogenic risk was observed for ß-HCH (Turkey and China), followed by α-HCH (Mexico). The highest non-carcinogenic risk was identified for Aldrin (all analyzed countries), followed by Dieldrin (Turkey) and γ-HCH (Mexico). The Monte Carlo analysis (under the assumption that γ-HCH has a normal distribution), the mean obtained was 8.22E-07 for children and 3.83E-07 for adults. This is in accordance with the standard risk assessment approach. In terms of percentiles, the Monte-Carlo approach indicates that 75% of child population is under the 1.07E-06 risk and 95% of adults under 7.35E-06.

A global systematic review, meta-analysis, and risk assessment of the concentration of vanadium in drinking water resources.

The presence of toxic metals such as vanadium in water resources has attracted considerable attention as a new concern in international health. Systematic review and meta-analysis were performed to assess the concentration of vanadium in water resources along with the relevant ecological risk assessment. Databases of Scopus, PubMed, and Embase were investigated to retrieve the related articles from January 01, 1974 to December 25, 2019. Twenty-eight articles containing 152 samples from 24 countries were included. Furthermore, the meta-analysis was conducted by the approach of z-score to estimate differences in the effect size. In addition, the mean of concentrations of vanadium was applied to calculate the risk assessment only to the water surface and choose the maximum environmental concentration (MEC) for demonstrate a worst-case scenario. Here, the risk assessment approach was used to show that the MEC of vanadium confirm the risk it for aquatic ecosystems, being fish (e.g., Danio rerio) our model organism due to their sensibility. According to findings, the MEC of vanadium in surface water varied from 0.010 µg L-1 (USA) and 68 µg L-1 (China), with an overall mean of 6.21 ± 13.3 µg L-1 (mean ± standard deviation). The ecological risk assessment demonstrated that people living in some countries such as China and Japan were at an adverse ecological risk of vanadium in the water resources. Hence, essential control plans besides adequate removal techniques must be implemented for significant deracination of heavy metals like vanadium.

Cerium-substituted magnetite: Fabrication, characterization and sonocatalytic activity assessment.

The present paper reports the sonocatalytic activity of cerium-substituted-magnetite for removal of oxytetracycline (OTC). The catalyst was prepared through a chemical route (co-precipitation, Fe3-xCexO4) and a mechanical procedure (CeO2/Fe3O4). Subsequently, the physico-chemical characteristics of both samples were determined using XRD, BET, SEM, EDX, TEM, Dot-mapping, FT-IR, DRS, and VSM analysis and compared to pristine magnetite and ceria. Afterwards, the effects of various operational conditions were assessed on sonocatalytic performance of Fe2.8Ce0.2O4 for OTC removal and the obtained optimal conditions were applied to compare the resulted DE with so-synthesized Fe3O4, CeO2, and CeO2/Fe3O4 samples. Fe2.8Ce0.2O4 (0.75 g/L) exhibited great catalytic performance for sono-degradation of OTC under its unchanged pH and US power of 300 W, wherein about 88% and 64% of OTC was removed at its initial concentrations of 20 and 50 mg/L. Moreover, the effects of the addition of a number of oxidants, organic and inorganic compounds and gases on the sonocatalytic degradation of OTC were evaluated under the identical condition. The obtained results presented an effective sonocatalytic system based on the synergistic action of Fe2.8Ce0.2O4 under ultrasonic irradiation.

Flow-injection chemiluminescence analysis for sensitive determination of atenolol using cadmium sulfide quantum dots.

A sensitive, rapid and simple flow-injection chemiluminescence (CL) system based on the light emitted from KMnO4-cadmium sulfide quantum dots (CdS QDs) reaction in the presence of cetyltrimethylammonium bromide (CTAB) in acidic medium was developed as a CL probe for the sensitive determination of atenolol. Optical and structural features of CdS QDs capped with l-cysteine, which synthesized via hydrothermal approach, were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL), and UV-Vis spectroscopy. The CL intensity of KMnO4-CdS QDs-CTAB was remarkably enhanced in the presence of trace level of atenolol. Under optimum experimental conditions, there is a linear relationship between the increase in CL intensity of KMnO4-CdS QDs-CTAB system and atenolol concentration in a range of 0.001 to 4.0 mg L(-1) and 4.0 to 18.0 mg L(-1), with a detection limit (3σ) of 0.0010 mg L(-1). A possible mechanism for KMnO4-CdS QDs-CTAB-atenolol CL reaction is proposed. To prove the practical application of the KMnO4-CdS QDs-CTAB CL method, the method was applied for the determination of atenolol in spiked environmental water samples and commercial pharmaceutical formulation. Furthermore, corona discharge ionization ion mobility spectrometry (CD-IMS) technique was utilized for determination of atenolol.